Canonical Allele Identifier: CA2686252417
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992908-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992908A>C , CM000670.2:g.16992908A>C GRCh38
NC_000008.10:g.16850417A>C , CM000670.1:g.16850417A>C GRCh37
NC_000008.9:g.16894788A>C NCBI36
NG_015978.1:g.14258T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*164T>G MANE Select ENSP00000180166.5:n.*164T>G
ENST00000180166.5:c.*164T>G ENSP00000180166.5:n.*164T>G
NM_019851.2:c.*164T>G NP_062825.1:n.*164T>G
NM_019851.3:c.*164T>G MANE Select NP_062825.1:n.*164T>G